ENST00000263207.8:c.2538G>A
MANE Select
|
ENSP00000263207.3:p.Lys846=
|
|
ENST00000263207.7:c.2538G>A
|
ENSP00000263207.3:p.Lys846=
|
|
ENST00000401994.5:c.2349G>A
|
ENSP00000384341.1:p.Lys783=
|
|
ENST00000406259.1:c.2520G>A
|
ENSP00000385444.1:p.Lys840=
|
|
ENST00000406522.5:c.2331G>A
|
ENSP00000384732.1:p.Lys777=
|
|
ENST00000495096.5:n.1460G>A
|
|
|
NM_001670.2:c.2538G>A
|
NP_001661.1:p.Lys846=
|
|
XM_005261242.1:c.2520G>A
|
XP_005261299.1:p.Lys840=
|
|
XM_005261243.3:c.2520G>A
|
XP_005261300.1:p.Lys840=
|
|
XM_005261244.3:c.2520G>A
|
XP_005261301.1:p.Lys840=
|
|
XM_006724243.1:c.2538G>A
|
XP_006724306.1:p.Lys846=
|
|
XM_006724245.2:c.2538G>A
|
XP_006724308.1:p.Lys846=
|
|
XM_006724246.2:c.2292G>A
|
XP_006724309.1:p.Lys764=
|
|
XM_006724247.2:c.2349G>A
|
XP_006724310.1:p.Lys783=
|
|
XM_006724248.2:c.2331G>A
|
XP_006724311.1:p.Lys777=
|
|
XM_011530179.1:c.2505G>A
|
XP_011528481.1:p.Lys835=
|
|
XM_011530180.1:c.2538G>A
|
XP_011528482.1:p.Lys846=
|
|
XM_011530182.1:c.1104G>A
|
XP_011528484.1:p.Lys368=
|
|
XM_011530183.1:c.1086G>A
|
XP_011528485.1:p.Lys362=
|
|
XR_937863.1:n.2625G>A
|
|
|
XR_937864.1:n.2625G>A
|
|
|
XM_005261242.3:c.2520G>A
|
XP_005261299.1:p.Lys840=
|
|
XM_005261243.4:c.2520G>A
|
XP_005261300.1:p.Lys840=
|
|
XM_005261244.4:c.2520G>A
|
XP_005261301.1:p.Lys840=
|
|
XM_006724243.3:c.2538G>A
|
XP_006724306.1:p.Lys846=
|
|
XM_006724245.3:c.2538G>A
|
XP_006724308.1:p.Lys846=
|
|
XM_006724246.4:c.2292G>A
|
XP_006724309.1:p.Lys764=
|
|
XM_006724247.4:c.2349G>A
|
XP_006724310.1:p.Lys783=
|
|
XM_006724248.4:c.2331G>A
|
XP_006724311.1:p.Lys777=
|
|
XM_011530179.3:c.2505G>A
|
XP_011528481.1:p.Lys835=
|
|
XM_011530182.3:c.1104G>A
|
XP_011528484.1:p.Lys368=
|
|
XM_011530183.3:c.1086G>A
|
XP_011528485.1:p.Lys362=
|
|
XM_024452249.1:c.2292G>A
|
XP_024308017.1:p.Lys764=
|
|
XR_937863.2:n.2625G>A
|
|
|
NM_001670.3:c.2538G>A
MANE Select
|
NP_001661.1:p.Lys846=
|
|